Medical devices are regulated by Ghana’s FDA (Food and Drug Authority). CLASSIFICATION SYSTEM:
Devices are classified according to the EU model of risk-based classification into Classes I, IIa, IIb, III, and IV. TIMEFRAME:
The approval process takes around 3-6 months for devices for all classes. LICENSE VALIDITY:
Licenses issued in Ghana are valid for three years. AUTHORIZED REPRESENTATIVE:
An authorized representative is required.
Last updated on January 22 2015.
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For more information on registration in Ghana, check out the following articles on our blog: Country at a Glance: Ghana